Device for determining the mass of a particle in suspension or in solution in a fluid

ABSTRACT

Device for determining the mass of a particle in suspension or in solution in a fluid. 
     Said device comprises: a first device ( 2 ) for the nebulization of the fluid ( 4 ) to obtain a flux comprising at least the particle, a second device ( 6 ) for the guidance and the aerodynamic focusing of the flux and a third device ( 12 ) for determining the mass of the particle by a frequency measurement, said third device comprising at least one gravimetric detector ( 14 ), arranged opposite the outlet of the second device, to receive the particle.

TECHNICAL FIELD

The present invention relates to a device for determining the mass of a particle in suspension or in solution in a fluid.

It applies in particular to mass spectrometry for species which are neutral or ionized.

STATE OF THE PRIOR ART

Conventional mass spectrometry (MS) is a universal chemical or biological analytical tool that is based on four essential components: an injection system, an ionization source, a mass analyser and an ion detector. These components are arranged in an enclosure, provided with pumps to create a vacuum therein.

The result of a mass spectrometry measurement is a spectrum that reflects the abundance, in a mixture, of a type of species as a function of the mass/charge ratio of said species. Each peak of the spectrum is the signature of a mono-charged or multi-charged ion; and the identification of species is achieved by means of a pre-established data bank.

The technique that has been described has now become a standard for numerous applications. However, it has a certain number of drawbacks:

-   -   this technique is relatively long to implement and it is not         very sensitive: a lot of biological material is necessary to         perform a measurement;     -   commercially available mass spectrometry devices are all         extremely bulky: they occupy a volume of the order of a few         cubic metres; and they are expensive: they cost several hundreds         of thousands of euros; and     -   this technique does not make it possible to measure important         masses which are typically above 100 kDa (1.66×10⁻²² kg), masses         for which the measurement resolution becomes completely         insufficient.

This latter drawback results mainly from the difficulty of accelerating sufficiently a heavy particle, and thus to give it sufficient energy so that it can reach the ion detector. It is however vital to be able to measure particles whose masses are greater than 100 kDa (1.66×10⁻²² kg), since they can have fundamental importance in the biomedical field: they may be for example viruses, bacteria, organelles, protein complexes or cells.

Another technique has been proposed for detecting masses using NEMS, in other words nano-electro-mechanical systems. And NEMS based resonant devices have been elaborated for which the detection limits are 10¹² times lower than those of QCM, in other words quartz crystal microbalances, which are commercially available. In this respect, reference may be made to the following documents:

-   K. L. Ekinci, X. M. H. Huang and M. L. Roukes, 2004, “Ultrasensitive     nanoelectromechanical mass detection”, Applied Physics Letters 84     (22): 4469. doi:10.1063/1.1755417 -   Michael L. Roukes and Kamil L. Ekinci, 2004, “Apparatus and method     for ultrasensitive nanoelectromechanical mass detection”, U.S. Pat.     No. 6,722,200

The principle of such a NEMS based resonating device is explained hereafter.

A particle of mass m_(p) settles on the NEMS, of stiffness k and of effective mass m, which increases its total mass. The new resonance frequency of the device is then equal to:

$f = {\frac{1}{2\pi}{\sqrt{\frac{k}{m + m_{p}}}.}}$

The frequency response peaks (in open loop), before and after deposition of the mass m_(p), are thus shifted by a quantity Δf, which is little different to

${{- \frac{m_{p}}{2m}} \cdot \frac{1}{2\pi}}{\sqrt{\frac{k}{m}}.}$

When the device is used in closed loop, its resonance frequency can thus be monitored in real time using electrical transduction means and loop closure means.

Thus, during its adsorption on a resonating NEMS, an individual particle of analyte, or a group of such particles, makes the resonance frequency of the NEMS drop sharply. And the mass of the particle, or the group of particles, may be deduced from the measurement of the frequency jump Δf.

Said frequency jump Δf depends on the mass of the particle, or the group of particles (see the value of Δf given above). But it also depends on the position at which the particle or the group of particles has settled on the surface of the NEMS. When it is not possible—and this is the most common case—to precisely locate the adsorption position of the particles on the NEMS, the frequency jump information alone is not sufficient. Recourse may then be made to a statistical approach, which consists:

-   -   in measuring a large number of events, each event corresponding         to the arrival of a single particle or a set of particles, said         arrival being associated with a frequency jump, and     -   in assuming an equiprobability of position on the surface of the         NEMS.

In this respect, reference may be made to the following document:

-   A. K. Naik, M. S. Hanay, W. K. Hiebert, X. L. Feng and M. L. Roukes,     2009, “Towards single-molecule nanomechanical mass spectrometry”,     Nature Nanotechnology 4: 445-450. doi:10.1038/NNANO.2009.152.

Another solution consists in measuring in real time the frequencies of two modes, or more, of the same NEMS. Several items of information are thereby available. In this respect, reference may be made to the following document:

-   S. Dohn, W. Svendsen, A. Boisen and O. Hansen, 2007, “Mass and     position determination of attached particles on cantilever based     mass sensors”, Review of Scientific Instruments 78: 103303.     doi:10.1063/1.2804074.

This mass measurement by means of NEMS has led to using them for performing mass spectrometry, which is then known as N EMS-MS. In this technique, the distribution of the masses of all the particles that are present in a mixture is measured and, to do so, they are sent one after the other onto the surface of a NEMS. This enables biological mass spectrometry, at the level of the individual particle, and procures the following advantages:

-   -   due to the integrability of NEMS which can be manufactured in         large quantities and in a collective manner on semiconductor         wafers, NEMS-MS is a technique that is highly parallelisable,         which makes the measurement very quick; and, it becomes possible         to envisage manufacturing portable and inexpensive NEMS-MS         devices;     -   the detection of mass using NEMS, which are gravimetric, is         sensitive both to ions and to neutral particles; the measurement         efficiency is thereby improved by several orders of magnitude;         and     -   gravimetric detection provides a mass resolution that is         constant over the whole measurement range, and thus provides an         excellent resolving power in high masses, unlike conventional         techniques.

FIG. 1 of the article of A. K. Naik et al., already cited, shows a known NEMS-MS system, the architecture of which is similar to those of conventional mass spectrometers: biological particles in liquid phase are injected and they are transmitted as efficiently as possible to a NEMS under vacuum, more precisely at a pressure of the order of 10⁻⁵ mTorr (10⁻⁶ Pa).

To do so, commercially available components are used: the injection source uses an ESI, in other words electrospray ionization, which nebulizes and ionizes the species to be analysed. The latter pass through several differential pumping and ionic guidance stages (using hexapoles), to finally arrive in the NEMS zone.

Such a known system has various drawbacks which do not enable the optimal use of all of the advantages brought by the NEMS-MS technique:

-   -   in this known system, the injection source and the NEMS are very         far apart from each other in order to enable differential         pumping; considerable losses of species between the source and         the NEMS ensue;     -   this distance apart imposes guiding the species to the NEMS; and         in this system, only ionized species are guided; neutral         particles are lost in the system; and     -   with such a distance apart, it is very difficult to focus a beam         of ions on a surface area less than a few square millimetres;         thus, a very low proportion of particles actually settles on the         NEMS, the surface area of which is typically of the order of a         few square micrometres.

All of these drawbacks make this known system very inefficient and do not make it possible to fully benefit from the advantages of NEMS-MS. In particular, the potential advantage that there would be in using a system dedicated to neutral and/or equally well ionized species may be seen. In fact, transmission by ion optics (and thus by means of electromagnetic fields) of generally heavy species, of the kind of those that are particularly targeted by NEMS-MS (organelles, viruses, bacteria, protein complexes, etc.), is very difficult. To transmit these massive particles with correct efficiency, it would be necessary to render them highly charged, which would have the effect of denaturing them and would no longer make it possible to measure them in their native state.

Resonating devices using NEMS are also known through the following documents:

-   WO 2012/034949, invention of S. Hentz -   WO 2012/034951, invention of S. Hentz et al. -   WO 2012/034990, invention of S. Hentz.

DESCRIPTION OF THE INVENTION

The aim of the present invention is to overcome the drawbacks of the known NEMS-MS system, described above, by associating a device for injecting neutral and/or ionized species, a guidance device, and a NEMS type detector, the whole favouring the proximity of these various components.

In a precise manner, the subject matter of the present invention is a device for determining the mass of at least one particle in suspension or in solution in a fluid, characterised in that it comprises:

-   -   a first device for the nebulization of the fluid, to obtain a         flux comprising at least said at least one particle,     -   a second device for the guidance and the aerodynamic focusing of         the flux, said second device comprising an inlet to receive the         flux, and an outlet, and     -   a third device for determining the mass of said at least one         particle by a frequency measurement, said third device         comprising at least one gravimetric detector, arranged opposite         the outlet of the second device, to receive said at least one         particle.

The device, the subject matter of the invention, thus makes it possible to determine the mass of each particle, in suspension or in solution, or a set of particles, depending on the flow rate of the flux used and the type of analyte containing the particles to be analysed. Obviously, “particle” is taken to mean an individual particle or an aggregate of particles.

According to a particular embodiment of the device, the subject matter of the invention, the second device is electrically neutral.

Such an electrically neutral device has the advantage of transmitting equally well positive ions and negative ions as well as neutral particles.

The second device may comprise an aerodynamic lens.

Said aerodynamic lens may be associated, at the outlet, with an orifice.

Preferably, the device, the subject matter of the invention, further comprises:

-   -   a zone at a given pressure, containing the first device, and     -   at least one vacuum enclosure, or first enclosure, provided to         be at a first pressure, below the pressure of said zone, the         first enclosure communicating with the zone and containing at         least one part of the second device.

“Given pressure” is taken to mean a pressure that may be an air pressure (atmospheric pressure) or a pressure of another gas, depending on the envisaged application for the invention.

Then, the second device may further comprise a capillary having an inlet orifice in the zone and an output orifice in the first enclosure, to place the zone in communication with the first enclosure.

In this case, the second device may comprise an aerodynamic lens opposite the inlet and/or outlet orifice of the capillary.

Thus, the concentration or focusing of the flux can take place equally well at the inlet and/or at the outlet of the capillary.

According to a particular embodiment, the device, the subject matter of the invention, further comprises another vacuum enclosure, or second enclosure, provided to be at a second pressure, which may be below the first pressure, said second enclosure containing the third device and communicating with the first enclosure via a first orifice opposite the gravimetric detector.

The gravimetric detector may be selected from nano-electromechanical systems, micro-electromechanical systems, quartz crystal microbalances, SAW (surface acoustic wave) resonators, BAW (bulk acoustic wave) resonators and impact detectors.

The first device may be selected from ultrasonic nebulizers, microwave induced nebulization devices, microcapillary array nebulizers and surface acoustic wave nebulizers.

BRIEF DESCRIPTION OF THE DRAWINGS

The present invention will be better understood on reading the description of embodiment examples given hereafter, purely as an indication and in no way limiting, and by referring to the appended drawings in which:

FIG. 1 is a schematic view of a particular embodiment of the device, the subject matter of the invention,

FIG. 2 illustrates schematically the principle of an aerodynamic focusing lens,

FIG. 3 illustrates schematically an example of a complete aerodynamic focusing system, and

FIG. 4 illustrates schematically and partially a simpler example of aerodynamic focusing device, which may be used in the present invention.

DETAILED DESCRIPTION OF PARTICULAR EMBODIMENTS

FIG. 1 is a schematic view of a particular embodiment of the device for determining the mass of a particle in suspension or in solution in a fluid, the subject matter of the invention. Said device comprises:

-   -   a device 2 for the nebulization of the fluid, namely an analyte         deposited in the form of droplet 4 in the example represented,         to obtain a flux comprising at least the particle,     -   a device for the guidance and the aerodynamic focusing of the         flux, said device comprising an aerodynamic focusing lens 6 in         which the inlet has the reference 8 and the outlet has the         reference 10, and     -   a device 12 for determining the mass of the particle by a         frequency measurement, said third device comprising at least one         gravimetric detector 14, arranged opposite the outlet 10 of the         aerodynamic focusing lens 6, to receive the particle.

As may be seen, the device represented in FIG. 1 also comprises:

-   -   a zone 16 at a given pressure, for example atmospheric pressure         (around 10⁵ Pa), said zone containing the nebulization device 2,         and     -   a vacuum enclosure 18 that communicates with the zone 16 and         contains the device 6 and in which a primary vacuum is         established, namely a residual pressure of the order of 10² Pa,         using a primary pump which is symbolised by the arrow 20.

The device for the guidance and the aerodynamic focusing of the flux also comprises a capillary (rectilinear) 22 having an inlet orifice 24 in the zone 16 and an output orifice 26 in the enclosure 18, to place the zone 6 in communication with said enclosure 18. The inlet of the device for the guidance and the aerodynamic focusing of the flux is constituted of the inlet orifice 24 of the capillary 22 and the outlet of said device for the guidance and the aerodynamic focusing of the flux is constituted of the outlet 10 of the aerodynamic focusing lens 6.

It is pointed out that the capillary 22 also makes it possible to desolvate the particles in suspension or in solution.

The device represented in FIG. 1 also comprises another vacuum enclosure 28 in which a secondary vacuum is established, namely a residual pressure of the order of 10⁻² Pa, by means of a turbomolecular pump which is symbolised by the arrow 30 (but, in other examples of the invention, the enclosures 18 and 28 could be at the same pressure).

The enclosure 28 contains the device 12 and communicates with the enclosure 18 via an orifice 32 opposite the detector 14.

Said detector 14 is mounted on a micro-positioning wafer 34, itself mounted on a sealed feed-through 36, as may be seen in FIG. 1.

The capillary 22 is aligned with said orifice 32, and the device 6 is comprised between the orifice 32 and the output orifice 26 of the capillary 22.

Thus, in the example of FIG. 1, the analytes are present in liquid phase and a portion of liquid is nebulized by the device 2, which produces an aerosol of very small droplets containing the analytes, mainly neutral, a part of which may potentially be ionized. Due to the pressure difference between the zone 16 and the enclosure 18, said aerosol is sucked into the input capillary 22. Opposite it is placed the aerodynamic focusing lens 6 which make it possible to guide equally well neutral species and ions to the detector 14, situated in the secondary vacuum enclosure 28.

The example of the invention, represented in FIG. 1, comprises two differential pumping chambers, namely the enclosures 18 and 28, but it is also possible to produce a device according to the invention comprising more than two differential pumping chambers, or even a single chamber.

In the example of FIG. 1, the detector 14 comprises a single NEMS but it is also possible to produce a device according to the invention where said detector comprises an array of such NEMS.

The means of reading and controlling the detector 14 are not represented. Said detector 14 may be temperature controlled, or not. The same is true of the inlet capillary 22.

It is advantageous to use a NEMS for the detection; but any other gravimetric detector (MEMS, QCM, SAW, BAW) may be used or, more generally, an inertial force detector, in particular an impact detector. With regard to the latter, reference may be made to the following document:

-   Jonghoo Park, Hua Qin, Mark Scalf, Ryan T. Hilger, Michael S.     Westphall, Lloyd M. Smith and Robert H. Blick, 2011, “A Mechanical     Nanomembrane Detector for Time-of-Flight Mass Spectrometry”, Nano     Letters 11: 3681-3684.

The aerodynamic focusing lens 6 is more simply known as “aerodynamic lens”. It is known that the latter is in fact composed of a series of elementary aerodynamic lenses. Examples of aerodynamic lenses are given hereafter.

In the invention, the use of such lenses makes it possible to guide in particular neutral species in order to maximise measurement efficiency. Thus, an electrostatic guidance of the kind of that employed in ion optics is not used.

It is recalled that an aerodynamic lens comprises a series of orifices that constitute elementary aerodynamic lenses. Said orifices may have identical sizes (see FIG. 3, to which we will return hereafter) or different sizes, for example decreasing sizes (see FIG. 2, to which we will return hereafter). Through these orifices, a diluted aerosol is sucked up. The majority of the carrier gas (and the majority of the water molecules sucked up by the capillary 22 used in the example of FIG. 1), gas which is light and free of particles, diffuses in the volume that is located at the outlet of the lens, whereas the heavy particles (compared to molecules of gas), such as biological molecules, acquire a sufficient momentum to be collected, via the outlet flux, in the form of a very fine jet. Under certain conditions, said jet may even be focused into a point (focal point).

Aerodynamic lenses are commonly used in mass spectrometers intended to measure particles present in aerosols but, in the latter case, said lenses are not used for the guidance and the focusing of particles to a detector since the species are always ionized following their introduction in a mass spectrometer: they are used for the concentration and the sorting of species to be measured, before their passage in the spectrometer.

In an elaborated form, a focusing device that can be used in the invention comprises (see FIG. 2) an inlet orifice 38, enabling the control of the flux and the differential pressure, and an aerodynamic lens 40 constituted of a series of elementary lenses 41. Said series of elementary lenses 41 makes it possible to compress the flux lines of particles as they progress along the device. At the outlet of the series of elementary lenses 41, an orifice 42 may be placed, making it possible to capture the collimated beam of heavy particles, whereas the light molecules (for example solvent molecules) have volume diffusion and escape.

In this respect, reference may be made to the following document:

-   US 2008/0022853, “Aerodynamic lens particle separator”, invention     of P. Ariessohn.

FIG. 3 illustrates schematically another example of aerodynamic focusing device, which may be used in the present invention and comprising an elementary aerodynamic lens or a series 43 of elementary aerodynamic lenses 44 and, at the outlet of said series of elementary lenses, a channel 45. Said channel 45 (or acceleration nose) may be a convergent channel or a convergent/divergent channel depending on the speed of the particles, and also helps the focusing of said particles

It is pointed out that only a part of the components of the device of FIG. 3 may be used in the invention. With regard to said device represented in FIG. 3, reference may be made to the technical documentation supplied by the firm Aerodyne Research, and particularly:

-   ARI Aerosol Mass Spectrometer, Operation Manual, page 9.

The aerodynamic lens 40 (respectively 43) of FIG. 2 (respectively FIG. 3) may obviously be associated with a capillary of the type of the capillary 22, placed at the inlet and/or at the outlet of said aerodynamic lens, or associated with an orifice of the type of the orifice 42 of FIG. 2.

FIG. 4 is a schematic and partial view of another device according to the invention, in which the aerodynamic focusing device is simply composed of the inlet capillary 22, of its output orifice 26 and of the inlet orifice 32 to the secondary vacuum enclosure 28 where the NEMS 14 is located. In this FIG. 4, the direction of circulation of the longitudinal fluxes is reversed compared to FIG. 1. And the arrows 48 represent a radial flux of light molecules at the outlet of the capillary 28.

In the invention, any type of nebulization device may be used, particularly an ultrasonic nebulizer, a microwave induced nebulization device or a microcapillary array nebulizer.

Advantageously, a SAWN is used, in other words a surface acoustic wave nebulizer. In this respect, reference may be made to the following document:

-   David R. Goodlett, Scott R. Heron and Jon Cooper, 2011, “Ions     generated by surface acoustic wave device detected by mass     spectrometry”, WO 2011/060369 A1.

It involves, in this case, using a surface acoustic wave resonator, on which a drop of liquid containing the analytes is deposited. The surface acoustic wave produced by the resonator dissipates its energy in the liquid which, then, is nebulized.

This nebulization method has the interest of only ionizing a very small part of the analytes, also with a very low ionization energy. In addition, it is capable of desorbing entire drops of water, as well as biological particles in a wide range of masses. In addition, such a nebulization device is integrable. It may be obtained by collective micro-manufacturing methods. And, it may be envisaged to integrate the entire architecture of the present invention when such an integrable device is used.

In the examples of the invention given above, the guidance and focusing device is electrically neutral. This signifies that no electromagnetic field is applied to said device or produced by it.

For the guidance and the focusing, preferably such an electrically neutral device is used. Nevertheless, a guidance and focusing device that is not electrically neutral could also be used, more precisely in which the lateral face is polarised with a certain voltage in order to separate the neutral species from the ionized species or, conversely, to polarise the device so as to obtain an electromagnetic field capable of focusing only the neutral species.

In the example of FIG. 1, the aerodynamic lens 6 is associated with the capillary 22. But an embodiment of the invention may also be envisaged in which the second device, serving for the guidance and for the aerodynamic focusing of the flux, comprises a diaphragm or an orifice in place of the capillary. 

1. Device for determining the mass of at least one particle in suspension or in solution in a fluid, comprising: a first device for the nebulization of the fluid to obtain a flux comprising at least said at least one particle, a second device for the guidance and the aerodynamic focusing of the flux, said second device comprising an inlet to receive the flux, and an outlet, and a third device for determining the mass of said at least one particle by a frequency measurement, said third device comprising at least one gravimetric detector, arranged opposite the outlet of the second device, to receive said at least one particle.
 2. Device according to claim 1, in which the second device is electrically neutral.
 3. Device according to claim 1, in which the second device comprises an aerodynamic lens.
 4. Device according to claim 3, in which the aerodynamic lens is associated, at the outlet, with an orifice.
 5. Device according to claim 1, further comprising: a zone at a given pressure, containing the first device, and at least one vacuum enclosure, or first enclosure, provided to be at a first pressure, below the pressure of said zone, the first enclosure communicating with the zone and containing at least one part of the second device.
 6. Device according to claim 5, in which the second device further comprises a capillary having an inlet orifice in the zone and an output orifice in the first enclosure, to place the zone in communication with the first enclosure.
 7. Device according to claim 6, in which the second device comprises an aerodynamic lens opposite the inlet and/or outlet orifice of the capillary.
 8. Device according to claim 1, further comprising another vacuum enclosure, or second enclosure, provided to be at a second pressure, optionally below the first pressure, containing the third device, and communicating with the first enclosure via a first orifice situated opposite the gravimetric detector.
 9. Device according to claim 1, in which the gravimetric detector is selected from nano-electromechanical systems, micro-electromechanical systems, quartz crystal microbalances, surface acoustic wave resonators, bulk acoustic wave resonators and impact detectors.
 10. Device according to claim 1, in which the first device is selected from ultrasonic nebulizers, microwave induced nebulization devices, microcapillary array nebulizers and surface acoustic wave nebulizers. 